Sparago A - Search Results

1

Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.

Sparago A, Cerrato F, Vernucci M, Ferrero GB, Silengo MC, Riccio A. Sparago A, et al. Nat Genet. 2004 Sep;36(9):958-60. doi: 10.1038/ng1410. Epub 2004 Aug 15. Nat Genet. 2004. PMID: 15314640

2

The two-domain hypothesis in Beckwith-Wiedemann syndrome: autonomous imprinting of the telomeric domain of the distal chromosome 7 cluster.

Cerrato F, Sparago A, Di Matteo I, Zou X, Dean W, Sasaki H, Smith P, Genesio R, Bruggemann M, Reik W, Riccio A. Cerrato F, et al. Among authors: sparago a. Hum Mol Genet. 2005 Feb 15;14(4):503-11. doi: 10.1093/hmg/ddi047. Epub 2005 Jan 7. Hum Mol Genet. 2005. PMID: 15640248

3

Mechanisms causing imprinting defects in familial Beckwith-Wiedemann syndrome with Wilms' tumour.

Sparago A, Russo S, Cerrato F, Ferraiuolo S, Castorina P, Selicorni A, Schwienbacher C, Negrini M, Ferrero GB, Silengo MC, Anichini C, Larizza L, Riccio A. Sparago A, et al. Hum Mol Genet. 2007 Feb 1;16(3):254-64. doi: 10.1093/hmg/ddl448. Epub 2006 Dec 11. Hum Mol Genet. 2007. PMID: 17158821

4

MS-MLPA is a specific and sensitive technique for detecting all chromosome 11p15.5 imprinting defects of BWS and SRS in a single-tube experiment.

Priolo M, Sparago A, Mammì C, Cerrato F, Laganà C, Riccio A. Priolo M, et al. Among authors: sparago a. Eur J Hum Genet. 2008 May;16(5):565-71. doi: 10.1038/sj.ejhg.5202001. Epub 2008 Jan 23. Eur J Hum Genet. 2008. PMID: 18212817

5

Different mechanisms cause imprinting defects at the IGF2/H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumour.

Cerrato F, Sparago A, Verde G, De Crescenzo A, Citro V, Cubellis MV, Rinaldi MM, Boccuto L, Neri G, Magnani C, D'Angelo P, Collini P, Perotti D, Sebastio G, Maher ER, Riccio A. Cerrato F, et al. Among authors: sparago a. Hum Mol Genet. 2008 May 15;17(10):1427-35. doi: 10.1093/hmg/ddn031. Epub 2008 Feb 1. Hum Mol Genet. 2008. PMID: 18245780 Free article.

6

Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer.

Murrell A, Ito Y, Verde G, Huddleston J, Woodfine K, Silengo MC, Spreafico F, Perotti D, De Crescenzo A, Sparago A, Cerrato F, Riccio A. Murrell A, et al. Among authors: sparago a. PLoS One. 2008 Mar 26;3(3):e1849. doi: 10.1371/journal.pone.0001849. PLoS One. 2008. PMID: 18365005 Free PMC article.

7

Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome.

Bliek J, Verde G, Callaway J, Maas SM, De Crescenzo A, Sparago A, Cerrato F, Russo S, Ferraiuolo S, Rinaldi MM, Fischetto R, Lalatta F, Giordano L, Ferrari P, Cubellis MV, Larizza L, Temple IK, Mannens MM, Mackay DJ, Riccio A. Bliek J, et al. Among authors: sparago a. Eur J Hum Genet. 2009 May;17(5):611-9. doi: 10.1038/ejhg.2008.233. Epub 2008 Dec 17. Eur J Hum Genet. 2009. PMID: 19092779 Free PMC article.

8

Inherited and Sporadic Epimutations at the IGF2-H19 locus in Beckwith-Wiedemann syndrome and Wilms' tumor.

Riccio A, Sparago A, Verde G, De Crescenzo A, Citro V, Cubellis MV, Ferrero GB, Silengo MC, Russo S, Larizza L, Cerrato F. Riccio A, et al. Among authors: sparago a. Endocr Dev. 2009;14:1-9. doi: 10.1159/000207461. Epub 2009 Feb 27. Endocr Dev. 2009. PMID: 19293570 Review.

9

Silver-Russell syndrome and Beckwith-Wiedemann syndrome phenotypes associated with 11p duplication in a single family.

Cardarelli L, Sparago A, De Crescenzo A, Nalesso E, Zavan B, Cubellis MV, Selicorni A, Cavicchioli P, Pozzan GB, Petrella M, Riccio A. Cardarelli L, et al. Among authors: sparago a. Pediatr Dev Pathol. 2010 Jul-Aug;13(4):326-30. doi: 10.2350/09-07-0686-CR.1. Pediatr Dev Pathol. 2010. PMID: 20028213

10

Disruption of genomic neighbourhood at the imprinted IGF2-H19 locus in Beckwith-Wiedemann syndrome and Silver-Russell syndrome.

Nativio R, Sparago A, Ito Y, Weksberg R, Riccio A, Murrell A. Nativio R, et al. Among authors: sparago a. Hum Mol Genet. 2011 Apr 1;20(7):1363-74. doi: 10.1093/hmg/ddr018. Epub 2011 Jan 31. Hum Mol Genet. 2011. PMID: 21282187 Free PMC article.

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